• Director, Trial Consent R&D - Iasi, Romania

    Job Locations RO-Iasi, Romania
    Job ID
    Information Technology
    Position Type
    Permanent Employee - Full-Time
  • Position Summary

    Director, Trial Consent R&D - Office base, Iasi Romania. Teams in Finland and Romania


    The role is responsible for development and management of a high-performing TrialConsent (eConsent) R&D that understands the SW development requirements, tools and processes in a regulated environment to reach maximum business velocity.

    Directs the company’s TrialConsent software development and technology research activities.

    Manages its software and technology development process and ensures continuous improvement of the development process, tools and methodologies.

    Directs TrialConsent research and development activities supporting continuity of the company’s technology platform for multiple products/solutions and ensures efficient use of companywide components, tools and practices deployment.

    Ensures product development activities alignment with company’s long-term strategy, strategic programs and product roadmaps.

    Provides technical assistance and leadership, when necessary.

    Works in close co-operation with other units inside and outside the R&D organisation to maximize cross unit synergies, such as business case development support for product management.


    • Contributes to the software and technology development processes and ensures continuous improvement of the development process and methodologies.
    • Ensures the TrialConsent product capabilities enable efficient, high performing and robust production infrastructure administration, maintenance and development.
    • Ensures the TrialConsent product delivery efficiency in CRF Operations and SaaS
    • Establishes and directs research programs pertaining to supporting continuity of the company’s technology platform and the development of new products and enhancements to existing products in the domain.
    • Ensures efficient escalation and support processes for TrialConsent R&D.
    • Remains abreast of current technical progress to ensure company’s products remain competitive.
    • Oversees the quality management process related to TrialConsent software and systems development.
    • Assists in establishment of company’s long-range product and product development goals and objectives. 
    • Manages personnel activities of staff, for example hiring, competence development and performance management.
    • Travel as necessary.
    • Other responsibilities will be assigned as required.


    • Minimum of ten years technical experience in a software research and development environment. 
    • Significant and successful experience of leading hi-tech sector R&D organization. Regulated industry is a plus. experience of leading in a multisite, multinational and multi geography hi-tech sector R&D organization. Regulated industry is a plus.
    • Experience in leading virtual teams and managing across a matrix.
    • Proven experience in R&D leadership for large, company-owned products/solutions, with multi-year lifespan.
    • Excellent practical Agile SW development and testing knowledge with modern SW engineering tools.
    • Excellent organizational, leadership and communications skills.
    • Must be able to deal effectively with all levels of the organization.
    • Results-oriented person with a “can do” attitude.


    About CRF Health

    Global Leader in eCOA Solutions




    CRF Health is a global leader in eCOA (electronic Clinical Outcome Assessments) solutions for the life sciences industry. eCOA encompasses PROs (Patient Reported Outcomes), ObsROs (Observer Reported Outcomes) and ClinROs (Clinician or Rater Reported Outcomes) with outstanding project management focused on delivering value for our customers.  Committed to driving the change to higher quality outcomes and more efficient paper-free clinical trials through improved patient engagement, our intuitive and patient-focused eCOA technology helps companies bring new medicines to market quickly, safely and more cost-effectively. Our complete eCOA solutions are ideal for home and site-based phase I-IV clinical trials across the world for many therapeutic areas and patient populations.  More information can be found on our website.  


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